A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004231



Internal ID21913574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132883699..132884743hg38UCSC Ensembl
chr9:135759086..135760130hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381045
hg191045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582562
Samples
Known GenesC9orf9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004231
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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